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The effect of heparin on lung function following cardiopulmonary bypass.

The effect of heparin on alveolar dead space following cardiopulmonary bypass.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12605000133639
Enrollment
30
Registered
2005-08-12
Start date
2004-11-30
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

A double blind randomised trial comparing intravenous heparin versus placebo (5% glucose). The infusion will be commenced 8 - 10 hours prior to commencement of surgery and ceased prior to the insertion of lines or sternotomy.

Sponsors

Nil
Lead Sponsor

Study design

Allocation
Randomised controlled trial
Intervention model
Single group
Primary purpose
Prevention
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Adult patients undergong elective cardiac surgery for coronary artery bypass grafting with cardiopulmonary bypass.

Exclusion criteria

Previous adverse reaction to heparin. Active bleeding. An additional surgical procedure to coronary artery bypass grafting planned. Creatinine >200umol/L.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026